Antioxidant Enzymes and Crude Mitochondria ATPases in the Radicle of Germinating Bean (Vigna unguiculata) Exposed to Different Concentrations of Crude Oil

The study examined the effect of Bonny Light whole
crude oil (WC) and its water soluble fraction (WSF) on the activities
of antioxidant enzymes (catalase (CAT) and superoxide dismutase
(SOD)) and crude mitochondria ATPases in the radicle of
germinating bean (Vigna unguiculata). The percentage germination,
level of lipid peroxidation, antioxidant enzyme and mitochondria
Ca2+ and Mg2+ ATPase activities were measured in the radicle of
bean after 7, 14 and 21 days post germination. Viable bean seeds
were planted in soils contaminated with 10ml, 25ml and 50ml of
whole crude oil (WC) and its water soluble fraction (WSF) to obtain
2, 5 and 10% v/w crude oil contamination. There was dose dependent
reduction of the number of bean seeds that germinated in the
contaminated soils compared with control (p<0.001). The activities
of the antioxidant enzymes, as well as, adenosine triphosphatase
enzymes, were also significantly (p<0.001) altered in the radicle of
the plants grown in contaminated soil compared with the control.
Generally, the level of lipid peroxidation was highest after 21 days
post germination when compared with control. Stress to germinating
bean caused by Bonny Light crude oil or its water soluble fraction
resulted in adaptive changes in crude mitochondria ATPases in the
radicle.





References:
[1] K-J. Dietz, “Redox-Dependent Regulation, Redox Control and
Oxidative Damage in Plant Cells Subjected to Abiotic Stress. In Plant
Stress Tolerance,” Methods and Protocols, Sunkar R. (ed), Humana
Press, Springer New York Dordrecht Heidelberg London, 2010. pp 57–
70.
[2] N. Merckl, R. Schutze-Kraft, and M. Arias, “Influence of fertilizer level
on phytoremediation of crude oil-contaminated soils with the tropical
grass Brachiaria brizantha (Hochst. ex A. Rich.) Stapf.” In:
Phytoremediation of petroleum-contaminated soil. Merkl, N. (Ed),
Margraf Publisher, Weikershim, 2005, pp 71-83
[3] C. I. Onuoha, A. E. Arinze, and A. E. Alaga, “Evaluation of growth of
some fungiin crude oil polluted environment,” Global Journal of Agr.
Sci., 2:1596-2903, 2003.
[4] J. G. Bundy, G. I. Paton, and C. D. Campbell, “Combined microbial
community level and single species biosensor responses to monitor
recovery of oil polluted soil,” Soil Biol. Biochem., 36(7):1149-1159,
2004.
[5] F. I. Achuba, and B. O. Peretiemo-Clarke, “Effect of spent engine oil on
soil catalase and dehydrogenase activities,” Int. Agrophysics, 22, 1-4,
2008.
[6] R. A. O. Odejimi, and O. Ogbalu, “Physiological Impact of Crude Oil
Polluted Soil on Growth, Carbohydrate and Protein Levels of Edible
Shoot of Fluted Pumpkin (Telfera occidentalis),” In: Botany and
Environmental Health, Akpan, G. and C.S.J.Odoemena
(Eds.).UniversityofUyo,Uyo,Nigeria, 2006, pp:102-105.
[7] G. Omosun, A. A. Markson, and O. Mbanasor, “Growth and Anatomy
of Amaranthus Hybridus as Affected by Different Crude Oil
Concentrations,” Am-Euras. J. Sci. Res., 3 (1): 70-74,2008.
[8] C. O. Adenipekun, “Bioremediation of engine oil polluted soil by
Pleurotus tuber regium Singer, a Nigerian whole-rot fungus,” Afri, J
Biotech. 7: 055-58, 2008
[9] C. Ortega-Villasante, R. Rellán-Álvarez, F. F. del Campo, R. O.
Carpena-Ruiz, and L. E. Hernández, “Cellular damage induced by
cadmium and mercury in Medicago sativa,”,” J Expt Bot.56: 2239–
2251, 2005.
[10] O. M. Adedokun, and A. E. Ataga, “Effects of amendments and
bioaugumentation of soil polluted with crude oil, automotive gasoline
oil, and spent engine oil on the growth of cowpea (Vigna unguiculata L.
Walp),” Scientific Res. Essay, 2(5):197-149, 2007.
[11] S. Siddiqui, and W. A. Adams, “The fate of diesel hydrocarbons in soils
and their effects on germination of perennial ryegrass,” Envtal Toxicol.,
17 (1): 49-62, 2002.
[12] O. O. Amund, and T. S. Akangou, “Microbial degradation of four
Nigerian crude oils in an estuarine microcosm,” Lett. Appl. Microbiol.
16: 118 – 121, 1993.
[13] G. Nicolotti, and S. Eglis, “Soil contamination by crude oil: impact on
the mycorrhizosphere and on the revegetation potential of forest trees,”
Envtal Pollu, 99: 37-43, 1998.
[14] M. Kontagora, “Address at an International Symposium on the National
Oil Spill Contingency Plan for Nigeria held at Badagri, Feb. 1991:1-3.
[15] J. A Rentz, B. Chapman, P. J. Alvarez, and J. L. Schnoor, “Stimulation
of hybrid poplar growth in petroleum-contaminated soils through
oxygen addition and soil nutrient amendments,” Intl J. Phytoremed. 5,
57–72, 2003.
[16] W. Aprill, and R. Sims, “Evaluation of the use of prairie grasses for
stimulating polycyclic aromatic hydrocarbon treatment in soil,”
Chemosphere. 20, 253–265, 1990.
[17] H. H. Liste, and M. Alexander, “Plant-promoted pyrene degradation in
soil,” Chemosphere 40, 7–10, 2000
[18] J. W. Anderson, J. M. Neff, B. A. Cox, H. E. Tatem, and G. M.
Hightower, “Characteristics of dispersions and water-soluble extracts of
crude oils and their toxicity to estuarine crustaceans and fish,” Mar.
Biol. 27: 75 – 88, 1974.
[19] J. M. C. Gutteridge, and C. Wilkins, “Copper dependent hydroxyl
radical damage ascorbic and formation of a thiobarbituric and reactive
products,” FEBS Lett., 137: 327 – 340, 1982
[20] K. A. Sinha, “Calorimetric assay of catalase,” Anal. Biochem. 47: 389 –
394, 1971.
[21] H. P. Misra, and I. Fridovich, “The role of superoixide ion in the
antioxidation of epinephrine and a simple assay for superoxide
dismutase,” J. Biol. Chem. 247: 3170 – 3175, 1972.
[22] R. D. Douce, J. Bourgurgnon, R. Brouguisse, and M. Neuburger,
“Isolation of plant mitochondria. General principles and criteria of
integrity,” Meth. Enzymol. 148: 403 – 409, 1987.
[23] R. Matsukama, and Tajikuchi, “Effects ofindomethsun on Ca2+
stimulated adenosine triphospahate in the synaptic vesicles of rat brain
in vitr,” Intl. J. Biochem. 14: 713 – 714, 1981.
[24] C. H. Fiske, and Y. Subarrow, “The colorimetric determination of
phosphorus,” J. Biol. Chem. 66: 375 – 400, 1925.
[25] O. H. Lowry, N. J. Rosebrough, A. L. Farr, and R. J. Randal, “Protein
measurement with folin-phenol reagent,” J. Biol. Chem. 193: 265 – 275,
1951.
[26] R. R. Sokal, and F. J. Rohlf, “The Principles and Practices of Statistics
in Biological Research,” Freeman and Co., San Francisco, 1969, pp.
469-484
[27] D. Tanyolac, Y. Ekmekci, and S. Unalan, “Changes in photochemical
and antioxidant enzyme activities in maize (Zea mays L.) leaves exposed
to excess copper,” Chemosphere, 67: 89–98, 2007.
[28] S. Gao, R. Yan, M. Cao, W. Yang, S. Wang, and F. Chen, “Effects of
copper on growth, antioxidant enzymes and phenylalanine ammonialyase
activities in Jatropha curcas L. seedling,” Plant Soil Environ., 54
(3): 117–122, 2008.
[29] O. M. Agbogidi, P. G. Eruotor, and S. O. Akparabi, “Effects of time of
application of crude oil to soil on the growth of maize (Zea mays L.),”
Res. J. Envtal Toxicol.., 1(3): 116-123, 2007.
[30] J. M. Ayotamuno, and R. B. Kogbara, “Determining the tolerance level
of Zea mays (maize) to a crude oil polluted agricultural soil,” Afri. J
Biotech., 6 (11), pp. 1332-1337, 2007.
[31] O. Blokhina, “Anoxia and Oxidative Stress: Lipid Peroxidation,
Antioxidant Status and Mitochondrial Functions in Plants”. Ph.D Thesis,
2000, University of Helsinki, Helsinki
[32] E. N. Edema, “Effect of produced water and water soluble fraction of
crude oil on Allium cepa,” J. Appl. Biosci. 30: 1866 – 1872, 2010.
[33] T. V. Chirkova, L. O. Novitskaya, and O. B. Blokhina, “Lipid
peroxidation and antioxidant systems under anoxia in plants differing in
their tolerance to oxygen deficiency,” Russian J. Plant Physiol. 45(1):
55-62, 1998.
[34] H. C. C. Maduka, “Effect of the time Course administration of Bergenin
on lipid peroxidation and some antioxidant defences during normal
biological oxidation reactions in weaning rats in vivo,” Nig. J. Bot., 21:
109 – 121, 2008.
[35] R. Mittler, “Oxidative stress, antioxidants and stress tolerance,” Trends
Plant Sci., 7: 405–410, 2002.
[36] R. M. Aitken, M. Palerson, H. Fisher, D. W. Buckingham, and M. Van
Duin, “Redox regulation of tyrosine phosphorylation in human
spermatozoa and its role in the control of human sperm function,” J Cell
Sc., 180: 2017 – 2005, 1995.
[37] G. E. Eriyamremu, S. O. Asagba, and K. Atoe, “Lipid peroxidation,
superoxide dismutase and mitochondria ATPases in the radicle of
germinating bean (Vigna unguiculata) exposed to different doses of
cadmium and lead,” Plant Archives. 7(1): 39-46, 2007.
[38] L. Taiz, and E. Zeiger, “Na+ Transport across the Plasma Membrane and
Vacuolar Compartmentation,” In: A Companion to Plant Physiology.
Fourth Edition. Sinauer Associates, Inc., Publisher. Sunderland, 2004.
[39] A. Vianello, F. Macri, E. Braidot, and E. N. Mokhova, “Effect of
cyclosporin A on energy coupling in pea stem mitochondria,” FEBS
Lett. 371: 258-260, 1995.
[40] P. Bernardi, K. M. Broekmeier, and D. R. Pfeiffer, “Recent progress on
regulation of the mitochondrial permeability transition pore: A
cyclosporin-sensitive pore in the inner mitochondrial membrane,” J.
Bioenerg. Biomembr. 26: 509-517,1994.
[41] P. Bernardi, and V. Petronilli, “The permeability transition pore as a
mitochondria calcium release channel: A critical appraisal,” J. Bioenerg.
Biomembr. 28: 131-138, 1996.
[42] F. Ichas, S. Jouaville, and J. P. Mazat, “Mitochondria are excitable
organelles capable of generating and conveying electrical and calcium
signals,” Cell, 89:1145-1153, 1997.